# Development of multiplex real-time PCR assays for differentiating SARS-CoV-2 from other respiratory and enteric pathogens

> **NIH FDA U18** · LOUISIANA STATE UNIV A&M COL BATON ROUGE · 2021 · $100,000

## Abstract

PROJECT SUMMARY/ABSTRACT
There is an urgent need for developing and validating new and improved molecular and
serological tests for the diagnosis of SARS-CoV-2 in companion animals (i.e., dogs and cats). It
has been shown that people with COVID-19 frequently pass SARS-CoV-2 on to their pets. Cats
are more susceptible to SARS-CoV-2 than dogs, and there is evidence that both species can
develop COVID-19 after a natural or experimental exposure. The clinical signs of COVID-19 in
cats and dogs include respiratory signs and diarrhea, which must be differentiated from feline
respiratory disease complex (FRDC), canine infectious respiratory disease complex (CIRDC or
commonly known as “kennel cough”), and diarrhea caused by other viruses, bacterial and
parasites. Thus, rapid detection and differentiation of SARS-CoV-2 from other common viral and
bacterial agents in a single specimen is critical in controlling COVID-19 and implementing
appropriate public health measures. Similarly, there is an urgent need for developing highly
specific and sensitive antibody detection (serological) assays to answer fundamental questions
about the epidemiology and immune response to SARS-CoV-2 and aid in the implementation and
evaluation of control programs. Thus, it is hypothesized that current laboratory testing for COVID-
19 in dogs and cats could be improved by developing new multiplex real-time qPCR/RT-qPCR
assays for the detection and differentiation of SARS-CoV-2 in respiratory (nasal and
nasopharyngeal) and fecal specimens, as well as developing a sandwich ELISA for the detection
of IgM and IgG immune responses using recombinant viral proteins. To test this central
hypothesis, we have two specific aims: Aim 1). Develop Multiplex Real-time PCR Assays to
Detect SARS-CoV-2 and Other Respiratory and Enteric Pathogens in Dogs and Cats: The
objective is to develop a series of multiplex (quadruplex) TaqMan® real-time qPCR/RT-qPCR
assays using a combination of fluorescently labeled probes. All assays will be optimized using
the new TaqPath 1-Step Multiplex Master Mix; and Aim 2). Develop Sandwich ELISA for the
Detection of Antibodies to SARS-CoV-2 in Dog and Cat Serum Samples: To detect IgM and IgG
immune response to SARS-CoV-2 in dogs and cats using recombinant nucleocapsid (N) and
spike (S) proteins. In summary, multiplex real-time qPCR/RT-qPCR assays are highly sensitive
and specific and will rapidly identify and distinguish dogs and cats infected with SARS-CoV-2.
The development and validation of both IgM and IgG ELISA will allow identifying animals exposed
to the virus. These newly developed assays will enhance the molecular and serologic diagnosis
of SARS-CoV-2 in pets, and also, advance epidemiological investigations.

## Key facts

- **NIH application ID:** 10449687
- **Project number:** 1U18FD007514-01
- **Recipient organization:** LOUISIANA STATE UNIV A&M COL BATON ROUGE
- **Principal Investigator:** Udeni B. R. Balasuriya
- **Activity code:** U18 (R01, R21, SBIR, etc.)
- **Funding institute:** FDA
- **Fiscal year:** 2021
- **Award amount:** $100,000
- **Award type:** 1
- **Project period:** 2021-09-15 → 2023-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10449687

## Citation

> US National Institutes of Health, RePORTER application 10449687, Development of multiplex real-time PCR assays for differentiating SARS-CoV-2 from other respiratory and enteric pathogens (1U18FD007514-01). Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/grant/nih/10449687. Licensed CC0.

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